HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → 3-Bromo-N-tert-butylbenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | m-Bromobenzenesulphonyl chloride | HCID 17943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-N-tert-butylbenzene-1-sulfonamide | HCID 4820926 | 1,248% |
Reaction Steps
tert-Butylamine (3.14 g, 3.0 mmol, 1.1 eq) and triethylamine (5.94 g, 58.6 mmol, 1.5 eq.) were dissolved in dichloromethane (20 mL) and stirred at room temperature while 3-bromobenzenesulfonyl chloride (10.0 g, 39.1 mmol) was added slowly. The mixture was stirred for 1 hour and then concentrated by evaporation under reduced pressure. The residue was taken up in 5% citric acid and ethyl acetate. The organic layer is washed repeatedly with brine and water, dried over anhydrous magnesium sulfate and concentrated to give N-tert-butyl-3-bromobenzenesulfonamide (10.94 g) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09162986B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-f24f1bb07fe44da88800c85cb0d62889 |
| Source note | uspto-grants-2015_10 |